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G-tube tips blog

July 7, 2024/by Niki Markou

Blog post G-Tube Tips for Lafora families

G-Tube Tips for Lafora Disease Patients

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https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png 0 0 Niki Markou https://chelseashope.org/wp-content/uploads/2022/02/ChelseasHope1.png Niki Markou2024-07-07 16:51:272024-07-08 08:04:43G-tube tips blog

About Chelsea’s Hope

Chelsea’s Hope began as a website in the fall of 2007 to share Chelsea Gerber’s story with family and friends. A 501(c)(3) organization since 2009, we have made an impact by raising awareness, connecting families worldwide, funding research, and maintaining hope. Our mission is to improve the lives of those affected by Lafora disease and help accelerate the development of treatments. [Read More]

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  • Open Letter to Noventia

  • New Team Members Join Chelsea’s Hope for the Summer

  • Announcing June 18th ION283 Q&A: What’s Next?

  • Chelsea’s Hope Advisory Board Meets to Discuss Research Goals

  • Announcing a Town Hall: Fully Funding the Safety Study

  • Read 2024 Impact in our Annual Report

  • Safety Study Update – February 2025

  • Chelsea’s Hope Earns Platinum Seal of Transparency for 2025

  • Chelsea’s Hope Welcomes 2025-2026 Board of Directors

  • In Memory of Dr. Joan Guinovart

The mission of Chelsea’s Hope is to improve the lives of those affected by Lafora Disease and help accelerate the development of treatments.

Chelsea’s Hope Lafora Children Research Fund is an IRS 501(c)3 non-profit organization. EIN: 27-1008382

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